Hydrochloric Acid

Hydrochloric Acid

SCHEMBL813315

Cc1cc(C)c(NCCN(C)CCNc2c(C(C)C)cccc2C(C)C)c(C)c1.[Cl-].[Cl-].[Co+2]

nearest known ligand 0.37

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.37
MEN1 O00255 2/20 0.37
LMNA P02545 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.35
GAA P10253 1/20 0.33
MAPK1 P28482 1/20 0.33
CRHR1 P34998 1/20 0.32
RAPGEF4 Q8WZA2 3/20 0.32
NLRP3 Q96P20 2/20 0.32

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Bromide SCHEMBL813250 0.97 MEN1 (0.37) KMT2AMEN1LMNASMN1; SMN2GAA
Hydrochloric Acid SCHEMBL813583 0.90 RAPGEF4 (0.32) KMT2ARAPGEF4
Hydrochloric Acid SCHEMBL813410 0.90 MEN1 (0.44) KMT2AMEN1LMNASMN1; SMN2MAPK1
Hydrochloric Acid SCHEMBL813625 0.89 MEN1 (0.37) KMT2AMEN1LMNASMN1; SMN2MAPK1
Hydrochloric Acid SCHEMBL813185 0.89 SMN1; SMN2 (0.42) KMT2AMEN1LMNASMN1; SMN2
Bromide SCHEMBL812800 0.87 MEN1 (0.44) KMT2AMEN1LMNASMN1; SMN2MAPK1
Bromide SCHEMBL814159 0.87 RAPGEF4 (0.32) RAPGEF4
Hydrochloric Acid SCHEMBL812453 0.87 SMN1; SMN2 (0.44) KMT2AMEN1LMNASMN1; SMN2
Bromide SCHEMBL815338 0.86 MEN1 (0.37) KMT2AMEN1LMNASMN1; SMN2MAPK1
Hydrochloric Acid SCHEMBL814755 0.86 RAPGEF4 (0.30) KMT2ARAPGEF4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8058372-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2011-11-15 US disclosed
US-20080319147-A1 Catalyst Composition II EXXONMOBIL CHEMICAL PATENTS INC. 2008-12-25 US disclosed
US-7371803-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2008-05-13 US disclosed
US-20070066776-A1 Catalyst composition II SOLAN GREGORY A 2007-03-22 US disclosed
US-7189791-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2007-03-13 US disclosed
EP-1641842-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND Exxonmobil Chemical Patents Inc. (US) 2006-04-05 EP disclosed
US-20040266961-A1 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. 2004-12-30 US disclosed
WO-2004106390-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND EXXONMOBIL CHEMICAL PATENTS INC. (US) 2004-12-09 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040266961-A1 Catalyst composition II MLX, CBX2, BMX KMT2A 530/4885MEN1 1095/4885LMNA 25/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.